{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Kadi",
      "state": "N/A",
      "country": "India",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73466",
      "recalling_firm": "Torrent Pharmaceuticals Limited",
      "address_1": "Ahmedabad Mehsana Highway",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0824-2016",
      "product_description": "Telmisartan Tablets, USP, 80 mg, 30-count (3 x 10 unit-dose blisters) per carton, Rx only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, Dist. Mehsana, INDIA.; For: Torrent Pharma Inc., 150 Allen Road, Suite 102, Basking Ridge, NJ 07920, NDC 13668-158-72, UPC 3 13668 158 72 4.",
      "product_quantity": "20,952 cartons",
      "reason_for_recall": "Presence of Foreign Substance: Product complaint for the presence of foreign matter identified as silicone within the tablet.",
      "recall_initiation_date": "20160225",
      "center_classification_date": "20160418",
      "termination_date": "20160603",
      "report_date": "20160427",
      "code_info": "Lot#: BBV8B002R, Exp 12/16"
    }
  ]
}